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「ethers」の共起表現(1語右で並び替え) - Weblio英語共起表現検索
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「ethers」の共起表現一覧(1語右で並び替え)

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hosphine) and assists the synthesis of esters, ethers, amines and thioethers of alcohols.
Hydrocarbon mixtures are composed of petroleum ethers and other hydrocarbons.
They can be easily protected with MTM ethers and recovered in good yield.
aliphatic hydrocarbons, ethyl acetate, glycol ethers, and acetone.
olvent properties of lower molecular weight of ethers and alcohols.
n eliminated completely, however such items as ethers and potions do appear in the game to be used o
s alcohols and carboxylic acids into the silyl ethers and silyl esters, respectively.
methyl compounds, particularly trifluoromethyl ethers and trifluoromethyl aromatics, are converted i
sed with the class of organic compounds called ethers; and equally, going under its alternative name
ted him to enter the domain of these superfine ethers, and become familiar with their mysteries.
int (175-325°C) than gasoline or the petroleum ethers, and a lower boiling point than the oils.
Ethers are slightly polar.
Crown ethers are useful as phase transfer catalysts.
3,4-Dimethoxybenzyl ethers are produced in the same ways.
Glycol ethers are a group of solvents based on alkyl ethers
Crown ethers are not the only macrocyclic ligands that have
Various silyl ethers are also popular protecting groups for several
toxic) mercuric chloride, to which most other ethers are stable.
polyphenyl and fluorinated ethers are the "raw materials" for Nye lubricants.
Ethers are more polar than alkenes but not as polar a
ohols give a substantial amount of alkenes and ethers as side products.
unctional molecules becomes possible using MTM ethers as the protective groups for their hydroxyl gr
e in the 1960s with the synthesis of the crown ethers by Charles J. Pedersen.
Depending on the substituents, some ethers can be cleaved with a variety of reagents, e.g
d for the production of perfluorinated amines, ethers, carboxylic acids, and sulfonic acids.
In contrast to crown ethers, cryptands bind the guest ions using both nitr
Like crown ethers, cyclen compounds are capable of selectively b
Unlike most ethers, does not form peroxides on storage
mediate in the synthesis of glycerol, glycidyl ethers, esters and amines.
f nucleophiles, including enolates, enol silyl ethers, Grignard reagents, organolithium reagents, al
Perhaps the most common use of halogenated ethers has been in anesthesiology.
MTM ethers have another advantage.
the synthesis and binding properties of crown ethers in a seminal series of papers.
eophiles and the use of triisopropylsilyl enol ethers in organic synthesis.
s are based on a formula containing diglycidyl ethers, including BADGE.
suggests that occupational exposure to glycol ethers is related to low motile sperm count in men, b
e Selexol solvent is a mixture of the dimethyl ethers of polyethylene glycol.
readily available commercially as solutions of ethers or hydrocarbons; it is not usually prepared in
The reaction of enolates, enol ethers, or enol acetates with NBS is the preferred me
iting the blending of gasoline with "alcohols, ethers, or other oxygenates."
Some ethers rapidly cleave with boron tribromide (even alu
options of anesthesiologists, but halogenated ethers remain a mainstay of general anesthesia.
Schedules I and II to include isomers, esters, ethers, salts of isomers, esters and ethers, and any
yl ether has the same properties as some other ethers, such as volatility, explosive vapors, and the
xplosions when tert-butyllithium is mixed with ethers such as diethyl ether, tetrahydrofuran, and gl
Ethers susceptible to this reaction, a typical exampl
reacts faster with t-butyldimethysilyl (TBDMS) ethers than triisopropylsilyl (TIPS) ethers.
the para-methoxybenzyl and 3,4-dimethoxybenzyl ethers, the former are generated by treatment of the
It also reacts with alcohols to give methyl ethers, where diazomethane may not.
are created by the reaction of P4S10 with aryl ethers which are different from anisole.
ids (RR'-O+-C-R'R) are prepared by reaction of ethers with diazo compounds.
Fatty alcohol polyglycol ethers with a narrow homolog distribution, which are
                                                                                                    


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